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DI-N-BUTYLDIBROMOTIN is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

996-08-7

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996-08-7 Usage

Safety Profile

Poison by ingestion. Moderately toxic by skin contact. See also TIN COMPOUNDS. When heated to decomposition it emits toxic fumes of Br-

Check Digit Verification of cas no

The CAS Registry Mumber 996-08-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,9 and 6 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 996-08:
(5*9)+(4*9)+(3*6)+(2*0)+(1*8)=107
107 % 10 = 7
So 996-08-7 is a valid CAS Registry Number.
InChI:InChI=1/2C4H9.2BrH.Sn/c2*1-3-4-2;;;/h2*1,3-4H2,2H3;2*1H;/q;;;;+2/p-2/rC8H18Br2Sn/c1-3-5-7-11(9,10)8-6-4-2/h3-8H2,1-2H3

996-08-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name dibromo(dibutyl)stannane

1.2 Other means of identification

Product number -
Other names Dibutyl tin dibromide

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:996-08-7 SDS

996-08-7Relevant academic research and scientific papers

Bromodestannylation reactions of some functionally substituted organotin compounds

Chopa, A. B.,Koll, L. C.,Podesta, J. C.,Mitchell, T. N.

, p. 283 - 296 (2007/10/02)

Bromodestannylation reactions are reported for several functional substituted organotin compounds in carbon tetrachloride and acetonitrile as solvents.The reactions in carbon tetrachloride proceed with a high degree of retention of configuration at the carbon involved in the electrophilic substitution, while in a polar solvent there is an increase in the amount of inversion product formed.The electrophilic cleavage in the β-trialkylstannyl esters takes place with a complete reversal of the normal sequence of Sn-C bond cleavage by halogens; this is explained by tin assistance.The configuration of some 3-trialkylstannylpropanenitriles, β-bromonitriles and β-bromoesters are assigned.Full, 1H, 13C and 119Sn NMR data are given.

A highly selective synthesis of R2SnX2 (R = alkyl, X = Br, Cl) species directly from tin and alkyl halides

Ugo, R.,Chiesa, A.,Fusi, A.

, p. 25 - 30 (2007/10/02)

The reaction : Sn + 2RX -> SnR2X2 (X = Cl, Br) occurs at relatively low temperature (80 - 120 degC) and with selectives as high as 95 - 99percent in the presence of catalytic system fored by a crown ether and potassium iodide.The reaction is favoured by aprotic dipolar solvents such as dimethylformamide; the presence of an alkyl iodide as cocatalyst has a positive effect, the selectivity remaining unchanged.

Production of organotin halides

-

, (2008/06/13)

A process is disclosed for the direct production of organotin halides, particularly triorganotin halides by the reaction of elemental tin and an organotin halide in the presence of a reagent amount of an `onium compound of the general formula Cat+ X-. Cat+ X- may represent a quaternary ammonium or phosphonium group or a ternary sulphonium group, or may also represent a complex of an alkali metal or alkaline earth metal with a polyoxygen compound. High yields of triorganotin halide product are obtained in contrast to results of reactions wherein Cat+ X- is present in only catalytic amounts.

Group 4 Organometallic Compounds. Part 8. Preparation and Moessbauer Spectra of Five- and Six-co-ordinate Di- and Tri-organotin Compounds containing Mixed Phenyl and Butyl Groups on Tin

Das, V. G. Kumar,Weng, Ng Seik,Smith, Peter J.,Hill, Robin

, p. 552 - 558 (2007/10/02)

Moessbauer spectroscopic data and preparative details are reported for a range of IVBuPh>, IVBu2Ph>, and IVBuPh2> compounds.The stereochemical preferences of the butyl and phenyl groups in octahedral and trigonal-

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